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BIO-STATISTICS

BIO-STATISTICS

PRECISE BIO-STATISTICS

Our biostatistics are the best , We aid you with operational and strategic statistics needed for every aspect of drug development. Are your legacy systems holding you back? We manage your design to implementation, integration, deployment and management. Are your legacy systems holding you back? We manage your design to implementation, integration, deployment and management.

Legacy to Modern applications

SKYYLIVES INFOTECH is your one stop shop for all your biostatistical reporting. Researchers often misinterpreted the statistical methods used in a study as they had a poor understanding of the statistical concepts. We assist our clients with complete support or augment your existing team. Our service structure provides your company the flexibility to obtain best-fit stats that aligns to your study and your business. We believe every stage in a clinical trial process needs the support of biostatisticians for design, development, management of data, data study, data analysis and for reporting reports. Whether your clinical trial is in the planning stage or an already existing trial, SKYYLIVES Infotech Data Science’s experienced and proficient biostatisticians can support you effectively.

  • Power analysis, definition of populations.
  • Analysis plans.
  • Contribute to CSR, ISS/ISE, DSUR, etc.
  • CDISC format deliverables
  • Power / Sample size estimation
  • Specification writing for SDTM, ADAM, TLF
  • Edit check programming for Data Management team
  • Statistical Analysis
  • SAS Programs Validation and QC of Reports
  • Protocol and SAP Preparation
  • Analysis dataset generation
  • Creating mock shell for Tables and Listings
  • Statistical analysis by using validated tools like SAS®
  • Generating tables, Listings and Graph (Safety and Efficacy)
We can source US-based Statistical Programmers and Global Statistical Programmers. All have been trained in CDISC and have experience as Statistical Programmers, All performing all the same tasks like generating datasets, up to and including specifications, and conversation of data standards and generating output.
Utilize our Statistical Programming expertise to enhance your clinical trials on every stage. We are through at analyzing clinical trial data to deliver concise and compliant outputs. A Project Manager will coordinate from inception to delivery, resource allocation, to timelines, budgets, and quality. Our Lead Programmers contribute in managing specific tasks on a subset of the project.
Our SAS programmers are always in demand as we ensure quality delivery, on time. QC Verification/Validation, SAS programming, Standard Operating Procedures (SOPs), and IT Projects are examples of the work typically performed by our experts.

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  • Email: [email protected]
  • Phone: 040-71327477